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Kresge Hearing Research Institute

Department of Otolaryngology

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Children's Hearing Laboratory

Publications

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• Publications
• Peer Review Electronic Publications
• Book Chapters
• Published Abstracts

Publications

• Chen W, Campbell CA, Green GE, Van Den Bogaert K, Komodikis C, Manolidis LS, Aconomou E, Kyamides Y, Christodoulou K, Faghel C, Giguere CM, Alford RL, Manolidis S, Van Camp G, Smith RJ. Linkage of otosclerosis to a third locus (OTSC3) on human chromosome 6. J Med Genet 39:473-477, 2002.
• Green GE, Scott DA, McDonald JM, Teagle HF, Tomblin BJ, Spencer LJ, Woodworth GG, Knutson JF, Gantz BJ, Sheffield VC, Smith RJ. Performance of cochlear implant recipients with GJB2-related deafness. Am J Med Genet 109:167-170, 2002.
• Ramakrishnan NA, Green GE, Pasha R, Drescher MJ, Swanson GS, Perin PC, Lakhani RS, Ahsan SF, hatfield JS, Khan KM, Drescher DG. Voltage-gates Ca(2+) channel Ca(V)1.3 subunit expressed in the hair cell epithelium of the sacculus of the trout Oncorhynchus mykiss: Cloning and comparison across vertebrate classes. Brain Res Mol Bran Res 30:109:69-83, 2002.
• Green GE, Mueller RF, Avraham KB, Cohn EB, Smith RJ. Audiologic Manifestations and features of Connexin 26 Deafness. J Aud Med, 2002 (in press).
• McGuirt WT, Prasad SD, Cucci RA, Green GE, Smith RJ. Clinical presentation of DFNB1. Adv Otorhinolaryngol 61:113-119, 2002.
• Green GE and Cunniff C. Genetic evaluation and counseling for congenital deafness. Adv Otorhinolaryngol 61:230-240, 2002.
• Campbell C, Cucci RA, Prasad S, Green GE, Edeal JB, Galer CE, Karniski LP, Sheffield VC, Smith RJ. Pendred syndrome, DFNB4, and PDS/SLC26A4: identification of eight novel mutations and possible genotype-phenotype correlations. Hum Mutation 17, 403-411 2001.
• Green GE, Northup K Hearing Preservation in Connexin 26 Deafness Otolaryngol Head Neck Surg 125, 274, 2001.
• Green GE, Smith RJ, Bent JP, and Cohn ES. Genetic testing to identify deaf newborns. JAMA 284, 1245, 2000.
• Green GE, Bauman NM, and Smith RJH. Pathogenesis and treatment of juvenile-onset recurrent respiratory papillomatosis. Otolaryngol Clin North Am 33, 187-207, 2000.
• Jun AJ, McGuirt WT, Hinojosa R, Green GE, Fischel-Ghodsian N, and Smith RJH. Temporal bone histopathology in Connexin 26-related hearing loss. Laryngoscope 110, 269-275, 2000.
• Prasad S, Cucci RA, Green GE, Smith RJ. Genetic testing for hereditary hearing loss: Connexin 26 (GJB2) allele variants and two novel deafness-causing mutations (R32C and 645-648delTAGA) and its allele variants. Hum Mutation 16, 502-508, 2000.
• Cucci RA, Prasad S, Kelley PM, Green GE, Storm K, Willcox S, Cohn ES, Van Camp G, and Smith RJ. The M34T allele variant of Connexin 26. Genet Testing 4, 335-344, 2000.
• Green GE, Scott DA, McDonald JM, Woodworth GG, Sheffield VC, and Smith RJH. Carrier rates in the mid-western United States for GJB2 mutations causing inherited deafness. JAMA 281, 2211-2216, 1999.
• McGuirt WT, Prasad SD, Griffith AJ, Kunst HP, Green GE, Shpargel KB, Runge C, Huybrechts C, Mueller RF, Lynch E, King MC, Brunner HG, Cremers CW, Takanosu M, Li SW, Arita M, Mayne R, Prockop DJ, Van Camp G, and Smith RJ. Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13). Nature Genetics 23, 413-419, 1999.
• Marsh JD, Lehman MH, Ritchie RH, Gwathmey JK, Green GE, and Schiebinger RJ. Androgen receptors mediate hypertrophy in cardiac myocytes. Circulation 98, 256-261, 1998.
• Green GE, Khan KM, Beisel KW, Drescher MJ, Hatfield JS, and Drescher DG. Calcium channel subunits in the mouse cochlea. Journal of Neurochemistry 67, 37-45, 1996.
• Drescher DG, Khan KM, Green GE, Morley BJ, Beisel KW, Kaul H, and Barretto RL. Analysis of nicotinic acetylcholine receptor subunits in the cochlea of the mouse. Comp Biochem Physiol 112C, 267-273, 1995.
• Green GE and Mathog RH. Microplating of frontal sinus fractures. Operative Techniques in Otolaryngology 6, 111-117, 1995.
• Drescher DG, Green GE, Khan KM, Hajela K, Biesel KW, Morley BJ, and Gupta AK. Analysis of g-aminobutyric acidA receptor subunits in the mouse cochlea by means of the polymerase chain reaction. Journal of Neurochemistry 61, 1167-1170, 1993.
• Green GE and Drescher DG. Detection of L-type, voltage-activated calcium channel subunits in the mouse cochlea by means of the polymerase chain reaction. Otolaryngol Head Neck Surg 109, 202, 1993.

Peer Review Electronic Publications

• Daley S, Tranebjaerg L, Samson RA, and Green GE. Jervell and Lange-Nielson Syndrome. In: GeneClinics: Clinical Genetic Information Resource [database online] Copyright, University of Washington, Seattle Available at http://www.geneclinics.org/ (Updated 07/29/2002)
• Green GE van Camp G, and Smith RJH. Hereditary hearing loss and deafness. In: GeneClinics: Clinical Genetic Information Resource [database online] Copyright, University of Washington, Seattle Available at http://www.geneclinics.org/ (Updated 02/14/1999).
• Green GE, Prasad S, and Smith RJH. Branchiootorenal syndrome. In: GeneClinics: Clinical Genetic Information Resource [database online] Copyright, University of Washington, Seattle Available at http://www.geneclinics.org/ (Updated 03/12/1999)

Book Chapters

• Green GE and Smith RJH Congenital hearing loss. In: Alper C, Eibling D, and Myers EN, eds Decision Making in Ear, Nose and Throat Disorders Orlando, FA: WB Saunders, 2001: 8-11.
• Green GE and Smith RJH Delineation of genetic components of communication disorders. In: Berger S Handbook of Genetic Communication Disorders San Diego: Academic Press; 2001: 11-29.
• Green GE, Biavati M and Smith RJH Laryngotracheal reconstruction with costal cartilage grafting. In: Hoffman HT, Funk G, McCulloch TM, and Graham SM, eds Iowa Head and Neck Protocols: Surgery, Nursing, and Speech-Language Pathology San Diego, California: Singular Publishing Group; 2000: 454-460.
• Green GE, Bauman NM, and Smith RJH Thyroglossal duct cyst excision. In: Hoffman HT, Funk G, McCulloch TM, and Graham SM, eds Iowa Head and Neck Protocols: Surgery, Nursing, and Speech-Language Pathology San Diego, California: Singular Publishing Group; 2000: 269-273.
• Green GE, Bauman NM, and Smith RJH Branchial cleft cyst/sinus/fistula excision. In: Hoffman HT, Funk G, McCulloch TM, and Graham SM, eds Iowa Head and Neck Protocols: Surgery, Nursing, and Speech-Language Pathology San Diego, California: Singular Publishing Group; 2000: 274-277.
• Green GE, Burke DM, and Smith RJH Pharmacotherapy for recurrent respiratory papillomatosis. In: Hoffman HT, Funk G, McCulloch TM, and Graham SM, eds Iowa Head and Neck Protocols: Surgery, Nursing, and Speech-Language Pathology San Diego, California: Singular Publishing Group; 2000: 114-117.
• Green GE, Bauman NM and Smith RJH Juvenile-onset recurrent respiratory papillomatosis. In: Ossoff, R, Shapshya S, Woodson G, and Netterville JL, eds The Larynx Philadelphia: Lippincott, Williams and Wilkins; 2002: 479-489.

Published Abstracts

• Green G.E. and The Connexin 26 Deafness Consortium. Hearing preservation in Connexin 26 deafness. Abstr. Assoc. Res. Otolaryngol. 22, 730, 2001.
• McGuirt W.T., Prasad S.D., Brown, M.R., Tomek M.S., Green G.E., Laer L.V., Smith S., Kenyon J.B., Van Camp G., and Smith R.J.H. Analysis of positional candidate genes for dominantly inherited nonsyndromic deafness, DFNA13. Abstr. Assoc. Res. Otolaryngol. 22, 730, 1999.
• Green G.E., Wayne S., Nishtala R., Chen A.H., Ramesh A., Srisailapathy C.R., Fukushima K., VanCamp G., and Smith R.J.H. Identification of a novel locus (DFNB19) for non-syndromic autosomal recessive hearing loss in a consanguineous family. Mol. Biol. Hear. Deaf. 3, 108, 1998.
• McGuirt W.T., Prasad S.D., Green G.E., Brown M.R., Tomek M.S., Van Laer L., Smith S., Kenyon J.B., VanCamp G., and Smith R.J.H. Fine mapping of the DFNA13 locus on chromosome 6p21.3 with construction of P1-derived artificial chromosomes and yeast artificial chromosomes. Mol. Biol. Hear. Deaf. 3, 102, 1998.
• Green G.E., Whitehead S., VanCamp G., and Smith R.J.H. Identification of a new locus -- DFNA19 -- for dominant hearing impairment. (1998) Mol. Biol. Hear. Deaf. 3, 107, 1998.
• McGuirt W.T., Fukushima K., Tomek M.S., Brown M.R., Green G.E., Mani S.R., Ramesh A., Srisailapathy C.R., Coucke P., Zbar R., Bell A., Willems P.J., VanCamp G., and Smith R.J.H. Evaluation of aggrecan as a candidate gene for otosclerosis. Mol. Biol. Hear. Deaf. 3, 170, 1998.
• Drescher D.G., Green G.E., Sheikhali S.A., Chomchai J.S., and Drescher M.J. Molecular analysis of a non-L-type voltage-gated calcium channel in a saccular hair-cell sheet. Mol. Biol. Hear. Deaf. 3, 20, 1998.
• Green G.E., Nguyen T.Q., Karpenko A.N., Chun W.J., Wang X., Drescher M.J., Sheikhali S. A., and Drescher D.G. Examination of the MSR III - MSR IV domain of a nicotinic alpha-9 like gene among vertebrates. Abstr. Assoc. Res. Otolaryngol. 21, 405, 1998.
• Green G.E., Lehman M.H., and Drescher D.G. Hearing impairment in patients with long QT syndrome. Abstr. Assoc. Res. Otolaryngol. 20, 730, 1997.
• Sheikhali S.A., Karadaghy A.A., Green G.E., and Drescher D.G. Non-L-type alpha-1 calcium channel subunit in a vertebrate hair cell sheet. Abstr. Soc. For Neurosci. 22, 423.17, 1997.
• Green G.E., Sheikhali S.A., Khan K.M., Drescher M.J., and Drescher D.G. Identification of calcium channel subunits expressed in a vertebrate hair cell sheet. Abstr. Assoc. Res. Otolaryngol. 19, 604, 1996.
• Khan K.M., Green G.E., Hatfield J.S., Shakir A.G., and Drescher D. G. RT-PCR subunit analysis and immunohistochemical localization of voltage-gated calcium channels in the mammalian cochlea. Abstr. Assoc. Res. Otolaryngol. 19, 605, 1996.
• Karadaghy A.A., Green G.E., Khan K.M. and Drescher D.G. Expression of an a9-like nicotinic acetycholine receptor subunit in teleost hair cells. Abstr. Assoc. Res. Otolaryngol. 19, 521, 1996.
• Kim S.Y., Drescher M.J., Baretto R.L., Green G.E., and Drescher D.G. Identification of mRNA for adenylyl cyclase isoforms VII and VIII in the mouse cochlea by RT-PCR. Abstr. Assoc. Res. Otolaryngol. 19, 737, 1996.
• Green G.E., Lehman M.H., and Drescher D.G. Dominant inheritance of hearing impairment in patients with Long QT syndrome. Am. J. Human Genetics. 57, A91, 1995.
• Green G.E. and Drescher D.G. Identification of a potassium channel gene - MERG - expressed in the mouse cochlea. Mol. Biol. Hear. Deaf. 2, 126, 1995.
• Drescher D.G., and Green G.E. Voltage-gated calcium channel subunits in the mouse cochlea. Mol. Biol. Hear. Deaf. 2, 90, 1995.
• Green G.E. and Drescher D.G. Identification of mRNA for heme oxygenase-2 in the mouse cochlea Abstr. Assoc. Res. Otolaryngol. 18, 569, 1995.
• Green G.E. , Drescher D.G., and Beisel K.W. Identification of a cardiac-type potassium channel expressed in the mouse cochlea. Abstr. Assoc. Res. Otolaryngol. 17, 320, 1994.
• Drescher M.J., Green G.E., and Lasak J.M. Adenylyl cyclase isoforms expressed in the mouse cochlea identified by polymerase chain reaction analysis. Abstr. Assoc. Res. Otolaryngol. 17, 319, 1994.
• Khan K.M., Green G.E., Gordon D., Gupta A.K., Drescher D.G. Detection of nicotinic receptor subunits in the mouse cochlea. Abstr. Assoc. Res. Otolaryngol. 17, 318, 1994.
• Green G.E., Drescher D.G. The mammalian cochlea expresses mRNA for subunits of the L-type calcium channel. Abstr. Assoc. Res. Otolaryngol. 23, 580.1, 1993.
• Chen K., Green G.E., Waller G.H., Drescher D.G., and Godfry D.A. Muscarinic receptor subtypes in rat cochlear nucleus. Abstr. Soc. for Neurosci. 23, 465.6, 1993.